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infantile myofibromatosis

Disease Summary
Associated Targets (2)
Tclin

1

Tchem

1


Explore Associated Targets
Mondo Description A benign, multifocal, nodular and well-circumscribed neoplasm usually seen as a congenital neoplasm or in the first year of life. It is characterized by a biphasic growth pattern and is composed of small, undifferentiated mesenchymal cells associated with branching thin-walled vessels and more mature neoplastic spindle cells with abundant eosinophilic cytoplasm in a collagenous stroma.
Disease Ontology Description A connective tissue benign neoplasm that is characterized by the development of benign tumors in the skin, striated muscles, bones, and in exceptional cases, visceral organs.
Mondo Term and Equivalent IDs
MONDO:0016824:  infantile myofibromatosis
GARD:0002998: 
MESH:D018224: 
NCIT:C3742: 
OMIMPS:228550: 
ONCOTREE:IMS: 
Orphanet:2591: 
UMLS:C0206648: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)